Please choose an event type to view the corresponding MedsFacts report:

COMPLETED SUICIDE ( 52 FDA reports)
DEATH ( 21 FDA reports)
POISONING ( 15 FDA reports)
CARDIO-RESPIRATORY ARREST ( 9 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COMA ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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